-
1
-
-
5044234361
-
Chromosome 21 and DS: From genomics to pathophysiology
-
Antonarakis SE, Lule R, Dermitzakis ET, Reymond A, Deutsch S 2004. Chromosome 21 and DS: From genomics to pathophysiology. Nat Rev Genet, 5: 725-738.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 725-738
-
-
Antonarakis, S.E.1
Lule, R.2
Dermitzakis, E.T.3
Reymond, A.4
Deutsch, S.5
-
2
-
-
33645539736
-
Down syndrome child with 48, XXY,+21 karyotype
-
Cyril C, Chandra N, Jegatheesan T, Chandralekha K, Ramesh A, Gopinath PM, Marimuthu KM 2005. Down syndrome child with 48, XXY,+21 karyotype. Indian Journal of Human Genetics, 11: 47-48.
-
(2005)
Indian Journal of Human Genetics
, vol.11
, pp. 47-48
-
-
Cyril, C.1
Chandra, N.2
Jegatheesan, T.3
Chandralekha, K.4
Ramesh, A.5
Gopinath, P.M.6
Marimuthu, K.M.7
-
3
-
-
0026604164
-
Identification of DNA sequences flanking the breakpoint of human t (14q21q). Robertsonian translocations
-
Earle E, Shaffer LG, Kalitsis P, McQuillan C, Dale S et al 1992. Identification of DNA sequences flanking the breakpoint of human t (14q21q). Robertsonian translocations. American Journal of Human Genetics, 50: 717-724
-
(1992)
American Journal of Human Genetics
, vol.50
, pp. 717-724
-
-
Earle, E.1
Shaffer, L.G.2
Kalitsis, P.3
McQuillan, C.4
Dale, S.5
-
4
-
-
0000261407
-
The chromosome in a pateient showing both mongolism and the Klinefelter syndrome
-
Ford CE, Jones KW, Miller OJ, Mittwoch U, Penrose LS, et al. 1959. The chromosome in a pateient showing both mongolism and the Klinefelter syndrome. Lancet, 1: 709-710.
-
(1959)
Lancet
, vol.1
, pp. 709-710
-
-
Ford, C.E.1
Jones, K.W.2
Miller, O.J.3
Mittwoch, U.4
Penrose, L.S.5
-
7
-
-
0027984566
-
Molecular Cytogenetic characterization of 17 rob (13q14q) Robertsonian translocations by FISH - narrowing the region containing the breakpoints
-
Han JY, Choo KHA, Shaffer LG 1994. Molecular Cytogenetic characterization of 17 rob (13q14q) Robertsonian translocations by FISH - narrowing the region containing the breakpoints. American Journal of Human Genetics, 55: 960-967.
-
(1994)
American Journal of Human Genetics
, vol.55
, pp. 960-967
-
-
Han, J.Y.1
Choo, K.H.A.2
Shaffer, L.G.3
-
9
-
-
0027379763
-
Paternal nondisjunction in trismoy 21: Excess of male patients
-
Petersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, et al. 1993. Paternal nondisjunction in trismoy 21: Excess of male patients. Human Molecular Genetics, 2: 1691-1695.
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 1691-1695
-
-
Petersen, M.B.1
Antonarakis, S.E.2
Hassold, T.J.3
Freeman, S.B.4
Sherman, S.L.5
-
10
-
-
0028147431
-
A somatic origin of homologous Robertsonian translocations and isochromosomes
-
Robinson WP, Bernasconi F, Basaran S, Yuksel-Apak M, Neri G, et al. 1994. A somatic origin of homologous Robertsonian translocations and isochromosomes. American Journal of Human Genetics, 54: 290-302.
-
(1994)
American Journal of Human Genetics
, vol.54
, pp. 290-302
-
-
Robinson, W.P.1
Bernasconi, F.2
Basaran, S.3
Yuksel-Apak, M.4
Neri, G.5
-
11
-
-
77953181653
-
Parental origin determination in thirty de novo Robersonian tanslocations
-
Schaffer LG, Jockson-Cook CK, Stasiowski BA, Spence JE, Brown JA 1992. Parental origin determination in thirty de novo Robersonian tanslocations. American Journal of Medical Genetics, 47: 383-386.
-
(1992)
American Journal of Medical Genetics
, vol.47
, pp. 383-386
-
-
Schaffer, L.G.1
Jockson-Cook, C.K.2
Stasiowski, B.A.3
Spence, J.E.4
Brown, J.A.5
-
13
-
-
77953186379
-
Personal communication
-
Verma IC 2006. Personal communication.
-
(2006)
-
-
Verma, I.C.1
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